FDA 510(k) Applications Submitted by MARK G URBANSKI

FDA 510(k) Number Submission Date Device Name Applicant
K990019 01/04/1999 DRG MEDIUM SCREW SYSTEM DOLPHIN MEDICAL TECHNOLOGIES, INC.
K960533 02/07/1996 K3 BONE SCREW SYSTEM KINETIKOS MEDICAL, INC.
K960537 02/07/1996 K2 BONE SCREW SYSTEM KINETIKOS MEDICAL, INC.
K960539 02/07/1996 DIAO HAND SURGERY SET KINETIKOS MEDICAL, INC.
K960692 02/20/1996 SUBTALAR MBA SYSTEM KINETIKOS MEDICAL, INC.
K961051 03/11/1996 UNIVERSAL TOTAL WRIST SYSTEM (MODIFICATION) KINETIKOS MEDICAL, INC.
K973810 10/07/1997 DRG LARGE SCREW SYSTEM DOLPHIN MEDICAL TECHNOLOGIES, INC.


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